Pressure Products Medical Device Manufacturing, LLC - FDA 510(k) Clea...
9
Total
9
Cleared
0
Denied
Pressure Products Medical Device Manufacturing, LLC has 9 FDA 510(k) cleared medical devices. Based in Morton, US.
Latest FDA clearance: Mar 2026. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pressure Products Medical Device Manufacturing, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Pressure Products Medical Device...
9 devices
Cleared
Mar 13, 2026
SafeSept RF Transseptal Guidewire (SSRF132
Cardiovascular
105d
Cleared
May 17, 2024
SafeSharp Transseptal Needle (CLICK071, CLICK171, CLICK098, CLICK198)
Cardiovascular
30d
Cleared
Sep 14, 2022
SafeSept® Transseptal Guidewire (SS-140)
Cardiovascular
93d
Cleared
Mar 05, 2021
SafeSept Blunt Needle
Cardiovascular
29d
Cleared
Oct 26, 2018
TSI Transseptal Introducer
Cardiovascular
191d
Cleared
Feb 21, 2018
TSN Transseptal Needle
Cardiovascular
148d
Cleared
Feb 16, 2018
Needle Free Transseptal Cannula
Cardiovascular
144d
Cleared
Dec 21, 2017
SafeSept Needle Free Transseptal Guidewire
Cardiovascular
90d
Cleared
Oct 20, 2017
SafeSept Transseptal Guidewire
Cardiovascular
228d